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  1. 1. How should Barrett’s oesophagus be defined and which patients should undergo regular surveillance? 2. Are there clinical features associated with increased cancer risk in Barrett’s oesophagus, which should influence the frequency of endo-scopic surveillance? 3. Are there diagnostic tools that should be uti-lised to screen the ...

  2. Proton pump inhibitors (PPIs) have the best clinical profile for symptomatic management (Recommendation grade A). Antireflux surgery is not superior to pharmacological acid suppression for the prevention of neoplastic progression of Barrett's oesophagus (Recommendation grade C).

  3. 16 sty 2023 · 23. Treatment of Refractory Barrett’s Esophagus. Although endoscopic eradication therapies as described above are very successful, there is a population of patients in whom complete eradication of Barrett’s esophagus cannot be achieved.

  4. 23 mar 2023 · The management of patients with Barrett’s esophagus still poses several clinical issues to the clinician, from correctly defining diagnosis to choosing adequate treatment. This brief and evidence-based review is aimed at providing a practical guide for the adequate management of this condition.

  5. 11 maj 2016 · If dysplasia or neoplasia is confirmed on endoscopy, treatment options include endoscopic mucosal resection or radiofrequency ablation. Barrett’s oesophagus is a premalignant condition where the oesophageal squamous epithelium undergoes columnar change with metaplasia which predisposes to the development of oesophageal adenocarcinoma.

  6. Barrett's oesophagus is more. 15 common in older age groups, men, people who are white and people who are. 16 overweight. The risk of progression to cancer is low. Fewer than 1% of people. 17 with Barrett’s oesophagus develop oesophageal adenocarcinoma each year.

  7. Surveillance in BE is aimed at early detection of dysplasia. Dysplasia is categorized as NDBE, indeterminate, LGD, HGD, or carcinoma [56]. The presence of dysplasia should be confirmed by a second pathologist expert in GI histopathology, due to a high degree of inter-observer variability [56].